Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Mohammed Ayman Al Khateeb"'
Autor:
Christiane Zweier, Saber Hamdan, Juliane Hoyer, André Reis, Arif B. Ekici, Karolin Eberlein, Dagmar Wieczorek, Ehab R. Abdelraouf, Tawfiq Froukh, Mandy Krumbiegel, Mohammed Ayman Al Khateeb, Mahmoud Fakher, Steffen Uebe, Sabine Hoffjan, Heinrich Sticht, Ahmad Abboud, Rebecca Buchert, Amina Ismael, Hasan Tawamie, Christian Thiel, Nagwa A. Meguid, Tim M. Strom, Judith Bauer, Ute Scheller, Ola H. Gebril, Rami Abou Jamra, Miriam S. Reuter, Safia Muhammad, Ebtessam Abdallah
Publikováno v:
JAMA psychiatry 74, 293-299 (2017)
Importance Autosomal recessive inherited neurodevelopmental disorders are highly heterogeneous, and many, possibly most, of the disease genes are still unknown. Objectives To promote the identification of disease genes through confirmation of previou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61f2d6d5387c23c13c872e743f96aa71
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85014729110
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=85014729110
Autor:
R Abou Jamra, Johannes Schumacher, Mohammed Ayman Al Khateeb, Steffen Uebe, Markus M. Nöthen, Lutz Priebe, Mahmoud Fakher, André Reis, Sigrun Wohlfart, Susanne Giesebrecht, Markus Zweier, Safia Muhammad, Arif B. Ekici, Saber Hamdan, Ahmad Abboud, Amina Ismael
Publikováno v:
European Journal of Human Genetics. 19:1161-1166
Non-specific intellectual disability of autosomal recessive inheritance (NS-ARID) represents an important fraction of severe cognitive dysfunction disorders. To date, only 10 genes have been identified, and further 24 linked-ARID loci have been repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2118baeb89244f4ec35cc0f452a7a6c7
https://doi.org/10.1038/ejhg.2011.98
https://doi.org/10.1038/ejhg.2011.98
